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M Baig

Showing results (161-170 of 184) with videos related to

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Human Genetics|October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing lossFarid Ullah, Waqar Rauf, Kamal Khan, et al.
Clinical Genetics|January 25, 2014
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndromeS Lohan, M Spielmann, S C Doelken, et al.
Genes|January 21, 2023
Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual DisabilityMaria Asif, Maryam Anayat, Faiza Tariq, et al.
Transboundary and Emerging Diseases|February 7, 2019
Phylogenetic analysis of haemagglutinin gene deciphering a new genetically distinct lineage of canine distemper virus circulating among domestic dogs in IndiaM Bhatt, K K Rajak, S Chakravarti, et al.
Mucosal Immunology|September 20, 2012
Human cervicovaginal mucus contains an activity that hinders HIV-1 movementS A Shukair, S A Allen, G C Cianci, et al.
Human Molecular Genetics|June 22, 2014
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani familyMuzammil A Khan, Verena M Rupp, Meritxell Orpinell, et al.
Nature Neuroscience|December 7, 2010
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessShahid M Baig, Alexandra Koschak, Andreas Lieb, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 23, 2023
Erdafitinib in BCG-treated high-risk non-muscle-invasive bladder cancerJ W F Catto, B Tran, M Rouprêt, et al.
Human Molecular Genetics|August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyMuhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
Cell Metabolism|April 9, 2013
Imbalance between neutrophil elastase and its inhibitor α1-antitrypsin in obesity alters insulin sensitivity, inflammation, and energy expenditureVirginie Mansuy-Aubert, Qiong L Zhou, Xiangyang Xie, et al.
Pageof 19

Showing results (161-170 of 184) with videos related to

Sort By:
Pageof 19
Human Genetics|October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing lossFarid Ullah, Waqar Rauf, Kamal Khan, et al.
Clinical Genetics|January 25, 2014
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndromeS Lohan, M Spielmann, S C Doelken, et al.
Genes|January 21, 2023
Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual DisabilityMaria Asif, Maryam Anayat, Faiza Tariq, et al.
Transboundary and Emerging Diseases|February 7, 2019
Phylogenetic analysis of haemagglutinin gene deciphering a new genetically distinct lineage of canine distemper virus circulating among domestic dogs in IndiaM Bhatt, K K Rajak, S Chakravarti, et al.
Mucosal Immunology|September 20, 2012
Human cervicovaginal mucus contains an activity that hinders HIV-1 movementS A Shukair, S A Allen, G C Cianci, et al.
Human Molecular Genetics|June 22, 2014
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani familyMuzammil A Khan, Verena M Rupp, Meritxell Orpinell, et al.
Nature Neuroscience|December 7, 2010
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessShahid M Baig, Alexandra Koschak, Andreas Lieb, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 23, 2023
Erdafitinib in BCG-treated high-risk non-muscle-invasive bladder cancerJ W F Catto, B Tran, M Rouprêt, et al.
Human Molecular Genetics|August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyMuhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
Cell Metabolism|April 9, 2013
Imbalance between neutrophil elastase and its inhibitor α1-antitrypsin in obesity alters insulin sensitivity, inflammation, and energy expenditureVirginie Mansuy-Aubert, Qiong L Zhou, Xiangyang Xie, et al.
Pageof 19